柠檬酸损害禾谷镰刀菌B型菌膜生物合成,但促进其生长和色素生物合成:转录组学和蛋白质组学分析。

IF 3.9 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Luzhou Cai, Ling Li, Dong Li, Yanping Wu, Jinrong Bai, Kai Zhong, Hong Gao
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引用次数: 0

摘要

谷草镰刀菌是一种致病性真菌,可引起毁灭性的植物疾病,如镰刀菌头疫病,导致严重的食物浪费,并因真菌毒素的积累对人类健康构成威胁。禾本科真菌是一种土传真菌,与植物和土壤密切相互作用,在复杂的环境中完成其生命周期。研究了植物根系分泌物和重金属螯合剂柠檬酸(CA)在2.5、5、10和20 mM浓度下对禾谷镰刀菌(F. graminearum)的影响。转录组学和蛋白质组学的综合分析发现,磷烯醇丙酮酸羧激酶(PEPCK)、Glpk和LAI12等碳源代谢相关酶的上调促进了真菌的生长,而负责产生金褐素和红褐素的聚酮类生物合成酶如AurF、AurJ和AurT则改变了菌丝色素。有趣的是,尽管真菌的生长得到促进,但许多Tri基因及其相应的蛋白质以及B型毛霉菌的生物合成都被显著下调。在本研究中,CK、2.5和5 mM组的RNA和蛋白表达模式相似,而10和20 mM组的RNA和蛋白表达模式相似。通过对CK、5和10 mM组的验证,CA作为B型毛霉烯生物合成抑制剂和生长促进剂的发现有望促进其合理应用,并为进一步研究防治禾粒赤霉病做出贡献。重要性:镰刀菌是一种具有挑战性的植物病原体,在世界范围内引起植物灾害,如小麦和玉米等小粮食作物的镰刀菌头疫病和穗腐病。此外,真菌对植物的入侵往往伴随着对健康有害的真菌毒素-毛霉烯的产生。因此,小麦赤霉病的防治一直是研究的热点。然而,目前,这些植物病害在世界范围内的流行和霉菌毒素积累超过安全限度表明有必要进行更多的相关研究。在过去的几十年里,研究人员试图确定与真菌生长、繁殖和霉菌毒素产生有关的关键物质,如碳源和氮源。有机酸由于其丰富的H+含量而一直被认为是抗真菌剂。然而,它们对真菌的综合影响很少被研究。本文主要研究了作物分泌物中常见的重金属螯合剂柠檬酸对禾谷镰刀菌代谢的影响。该结果有望为进一步研究植物-土壤-真菌相互作用及柠檬酸在农业中的合理利用提供理论依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Citric acid impairs type B trichothecene biosynthesis of Fusarium graminearum but enhances its growth and pigment biosynthesis: transcriptomic and proteomic analyses.

Fusarium graminearum is a pathogenic fungus that causes devastating plant diseases such as Fusarium head blight, leading to significant food waste and posing a threat to human health due to the accumulation of mycotoxins. As a soil-borne fungus, F. graminearum interacts closely with plants and soil, completing its life cycle in an intricate environment. In this investigation, citric acid (CA), a plant root exudate and heavy metal chelator, was investigated for its effect on F. graminearum at concentrations of 2.5, 5, 10, and 20 mM. The fungus treated with this CA gradient exhibited different growth conditions and mycelial colors. Integrative analysis of transcriptomics and proteomics found that the growth of the fungus was accelerated by the upregulation of carbon source metabolism-related enzymes such as phosphoenolpyruvate carboxykinase (PEPCK), Glpk, and LAI12, and the mycelial pigments were altered by polyketide biosynthetic enzymes like AurF, AurJ, and AurT, which were responsible for the production of aurofusarin and rubrofusarin. Interestingly, many Tri genes and their corresponding proteins along with type B trichothecene biosynthesis were significantly downregulated, though the fungal growth was promoted. In this study, the CK, 2.5, and 5 mM groups had similar expression patterns of RNA and protein, while the 10 and 20 mM groups were alike. With the validation of CK, 5, and 10 mM groups, the discovery of CA as a type B trichothecene biosynthesis inhibitor and growth promoter was expected to facilitate its reasonable application and contribute to further research for the prevention of F. graminearum.

Importance: Fusarium graminearum is a challenging phytopathogen that causes plant disasters worldwide, such as Fusarium head blight and ear rot in small grain crops like wheat and maize. Besides, the invasion of the fungus on plants is often accompanied by the production of health-threatening mycotoxins-trichothecenes. Therefore, the control of Fusarium graminearum has always been a hot area of research. However, currently, the prevalence of these plant diseases around the world and the mycotoxin accumulation beyond safety limits indicate the necessity for more related research. In the last decades, researchers have sought to identify the key substances associated with the growth, propagation, and mycotoxin production of the fungus, such as carbon and nitrogen sources. Organic acids have always been considered antifungal agents due to their abundant H+ content. However, their comprehensive impact on fungi has been rarely investigated. This research focused on the effect of citric acid, a type of crop exudate and a common heavy-metal chelator, on the metabolism of Fusarium graminearum. The result was expected to provide a theoretical basis for further studies on plants-soil-fungi interactions and the reasonable utilization of citric acid in agriculture.

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来源期刊
Applied and Environmental Microbiology
Applied and Environmental Microbiology 生物-生物工程与应用微生物
CiteScore
7.70
自引率
2.30%
发文量
730
审稿时长
1.9 months
期刊介绍: Applied and Environmental Microbiology (AEM) publishes papers that make significant contributions to (a) applied microbiology, including biotechnology, protein engineering, bioremediation, and food microbiology, (b) microbial ecology, including environmental, organismic, and genomic microbiology, and (c) interdisciplinary microbiology, including invertebrate microbiology, plant microbiology, aquatic microbiology, and geomicrobiology.
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